OLUX-E

Product NDC

40076-101

11-digit product format

400760101

Labeler code

40076

Product ID

40076-101_8a393f5a-e1aa-41f7-af41-73546eaa9529

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

clobetasol propionate

Dosage form

AEROSOL, FOAM

Route

TOPICAL

Labeler

Prestium Pharma, Inc.

Application

NDA022013

Marketing category

NDA

Marketing start

2007-02-12

Marketing end

2020-07-31

Substance

CLOBETASOL PROPIONATE

Active strength

1 mg/g

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record